GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metY in Cereibacter sphaeroides ATCC 17029

Align O-acetylhomoserine sulfhydrylase (EC:2.5.1.49) (characterized)
to candidate WP_011841100.1 RSPH17029_RS07895 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= reanno::Korea:Ga0059261_3194
         (402 letters)



>NCBI__GCF_000015985.1:WP_011841100.1
          Length = 397

 Score =  230 bits (587), Expect = 5e-65
 Identities = 133/343 (38%), Positives = 195/343 (56%), Gaps = 5/343 (1%)

Query: 54  ARFSGDQQGMTYSRLQNPTVEMLEQRIALLEGAEACRATASGMAAMTAALLCQLSAGDHL 113
           A+++G  +G TY+R  +P  E+L ++I  LEGAE      SGMAA+ A LL  L AGDH+
Sbjct: 45  AQYAGQVKGFTYAREGHPNAEVLARKIDALEGAEGGIVVGSGMAAVAAVLLGLLRAGDHV 104

Query: 114 IGGRAAFGSCRWLTDTQLPKFGIETTVVDARDPQQFIDAIRPNTKVFFFETPANPTMDVV 173
           +GG   +G    +    LP+ GI T++ DA D      A+RP TK+   E  +NPT+ V 
Sbjct: 105 VGGDQLYGRSLRMMAEDLPRLGIATSLADATDAAAVEAALRPETKLVLIEVVSNPTLRVA 164

Query: 174 DLKAVCAIARERGIVTVVDNAFATPALQRPMDFGADVVAYSATKMMDGQGRVLAGAV-CG 232
           DL  + A+ R RGI+  VD+ F+TP   RP D GAD+V +S TK++ G   V  G V C 
Sbjct: 165 DLDGIAALCRARGILLAVDSTFSTPRGIRPFDHGADIVIHSVTKLLAGHSDVTLGYVACR 224

Query: 233 TEEFINNTLLPFHRNTGPTLSPFNAWVVLKGLETLDLRIQRQSENALKVARFLEG--RVP 290
           T E +   +  F   TG T SPF+ W+  +GL +  LR  R  E A ++A  L G   V 
Sbjct: 225 TAE-LRRAVELFAVTTGLTPSPFDCWLAERGLLSFHLRYDRAEETAARLADHLAGLPGVR 283

Query: 291 RVNFPGLPSHPQHNLAMSQMA-AAGPIFSIELDGGRTQAHGLLDALGLIDISNNIGDSRS 349
           RV +P    HP    A++ +    G + S EL+GGR  A+ L  A+  +  +  +GD  +
Sbjct: 284 RVIYPLRADHPDQARAVALLGRRGGNMLSFELEGGRAAANALTRAMPAVAFAPTLGDVGT 343

Query: 350 LMTHPASTTHSGVAEDQRLLMGVGEGMLRLNVGLEDPEDLIAD 392
            ++HPAS++H  VA + R  +G+ EG  R++VG+E+ + LI D
Sbjct: 344 TLSHPASSSHRAVAPEVRARLGISEGFFRISVGVEEADLLIRD 386


Lambda     K      H
   0.319    0.134    0.396 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 352
Number of extensions: 12
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 402
Length of database: 397
Length adjustment: 31
Effective length of query: 371
Effective length of database: 366
Effective search space:   135786
Effective search space used:   135786
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 16 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory